ARTG 219979Probe, stimulator
ARTG ID: 219979 · Algostim Research & Development Pty Limited · Algotec Research and Development Ltd · Class IIa · Started February 07, 2014
Good Name: Algostim Research & Development Pty Limited - Probe, stimulator
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 219979
- Start Date
- February 07, 2014
- Effective Date
- February 07, 2014
- Country
- United Kingdom
- Address
- Basepoint Business Centre John de Mierre House Bridge Rd, Haywards Heath, West Sussex, RH16 1UA
PENS therapy Probes are sterile for single use and are used in conjunction with an Algotec PENS therapy device. A re-usable, non-sterile Intermediate Cable is the interface between the Probe and the Device. Probes are intended for the transfer of electrical stimulus, generated from the Algotec PENS therapy device and delivered to peripheral nerves. The stimulation field remains local to the Probe, the stimulation source, therefore larger areas may require the use of a longer length Probe, two Probes or a repeated procedure. PENS therapy probes are only intended for use by a trained physician and only in a clinical setting.
Access comprehensive regulatory information for Probe, stimulator in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 219979 and sponsored by Algostim Research & Development Pty Limited, manufactured by Algotec Research and Development Ltd in United Kingdom. The device registration started on February 07, 2014.
This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.